Osteosarcoma arising from osteochondroma of the tibia: case report and cytogenetic findings


Autoria(s): Engel, E. E.; Nogueira-Barbosa, M. H.; Brassesco, M. S.; Silva, G. E. B.; Valera, E. T.; Peria, F. M.; Motta, T. C.; Tone, L. G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

04/11/2013

04/11/2013

2012

Resumo

Osteochondroma is a cartilage capped benign tumor developing mainly at the juxta-epiphyseal region of long bones. The rate of malignant transformation, mainly into chondrosarcoma, is estimated to be less than 1-3%. Transformation into osteosarcoma is very rare and has been reported only thirteen times. There is little information on treatment and outcome. We report the case of a secondary osteosarcoma arising in the left tibia of a 23-year-old male, 10 years after the initial diagnosis of osteochondroma and after two partial resections. Malignant transformation occurred at the stalk and not at the cartilage cap, as would normally be expected. Chromosome banding analysis revealed the karyotype: 46,XY, t(3;13)(q21;q34) [2]/46,XY [18]. Records from additional cases will help determine the parameters that define these rare secondary bone lesions.

Sao Paulo State Research Foundation (FAPESP)

FAPESP (Sao Paulo State Research Foundation) [07/54236-4, 06/04827-3]

Identificador

GENETICS AND MOLECULAR RESEARCH, RIBEIRAO PRETO, v. 11, n. 1, supl. 1, Part 3, pp. 448-454, JUN, 2012

1676-5680

http://www.producao.usp.br/handle/BDPI/40815

10.4238/2012.March.1.1

http://dx.doi.org/10.4238/2012.March.1.1

Idioma(s)

eng

Publicador

FUNPEC-EDITORA

RIBEIRAO PRETO

Relação

GENETICS AND MOLECULAR RESEARCH

Direitos

openAccess

Copyright FUNPEC-EDITORA

Palavras-Chave #OSTEOSARCOMA #BONE NEOPLASMS #OSTEOCHONDROMA #SOLITARY OSTEOCHONDROMA #CHONDROSARCOMAS #EXOSTOSES #TUMORS #BIOCHEMISTRY & MOLECULAR BIOLOGY #GENETICS & HEREDITY
Tipo

article

original article

publishedVersion